Online Essential: Medical Device Regulation
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EEN LIVESTREAM OVER MEDICAL DEVICE REGULATION
In mei 2021 trad de nieuwe Medische Hulpmiddelen Verordening (MDR) in voege. Ruth Beckers brengt jou in heldere taal up to date over deze regelgeving.
Tijdens de livestream op 29 maart bespreekt Ruth volgende onderwerpen:
- Medical Device wetgevend kader
- Belangrijkste wijzigingen sinds mei 2021
- Medical Device Regulatory Process
- Introductie tot specifieke MDR vereisten
Deze livestream is specifiek voor HealthTech start-ups maar staat open voor iedereen die een update nodig heeft over de regelgeving rond medische hulpmiddelen.
Ruth Beckers is lange tijd actief in de MedTech sector. In 2015 richtte ze haar eigen Quality and Regulatory Affairs (QA/RA) dienstenbedrijf Qualix op. Het team van Qualix ondersteunt zowel start-ups als middelgrote tot grote organisaties actief in medische hulpmiddelen op het vlak van MDR.
Op het einde van de sessie is er ook tijd voor Q&A.
![slide6.png](https://www.bhic.care/sites/default/files/styles/paragraphspeaker/public/2022-09/slide6.png?h=02666105&itok=1ot8FG8o)
Ruth is al heel haar carrière actief in de MedTech sector. Zij richtte in 2015 haar eigen Quality and Regulatory Affairs (QA/RA) dienstenbedrijf Qualix op. Het team van Qualix werkt zowel voor start-ups als middelgrote tot grote organisaties actief in medische hulpmiddelen.